Khodyreva S, Dyrkheeva N, Lavrik O
Biomedicines. 2025; 12(12.
PMID: 39767715
PMC: 11673744.
DOI: 10.3390/biomedicines12122808.
Sledzinski P, Nowaczyk M, Smielowska M, Olejniczak M
BMC Biol. 2024; 22(1):282.
PMID: 39627841
PMC: 11616332.
DOI: 10.1186/s12915-024-02079-6.
Polyzos A, Cheong A, Yoo J, Blagec L, Toprani S, Nagel Z
Nat Commun. 2024; 15(1):7726.
PMID: 39231940
PMC: 11375129.
DOI: 10.1038/s41467-024-51906-5.
Foret M, Orciani C, Welikovitch L, Huang C, Cuello A, Do Carmo S
Commun Biol. 2024; 7(1):861.
PMID: 39004677
PMC: 11247100.
DOI: 10.1038/s42003-024-06552-4.
Ramadoss G, Namaganda S, Hamilton J, Sharma R, Chow K, Macklin B
bioRxiv. 2024; .
PMID: 38979269
PMC: 11230251.
DOI: 10.1101/2024.06.25.600517.
A Unifying Hypothesis for the Genome Dynamics Proposed to Underlie Neuropsychiatric Phenotypes.
Gericke G
Genes (Basel). 2024; 15(4).
PMID: 38674405
PMC: 11049865.
DOI: 10.3390/genes15040471.
Mobile circular DNAs regulating memory and communication in CNS neurons.
Smalheiser N
Front Mol Neurosci. 2023; 16:1304667.
PMID: 38125007
PMC: 10730651.
DOI: 10.3389/fnmol.2023.1304667.
New Facets of DNA Double Strand Break Repair: Radiation Dose as Key Determinant of HR versus c-NHEJ Engagement.
Mladenov E, Mladenova V, Stuschke M, Iliakis G
Int J Mol Sci. 2023; 24(19).
PMID: 37834403
PMC: 10573367.
DOI: 10.3390/ijms241914956.
Discovery of a 53BP1 Small Molecule Antagonist Using a Focused DNA-Encoded Library Screen.
Shell D, Foley C, Wang Q, Smith C, Guduru S, Zeng H
J Med Chem. 2023; 66(20):14133-14149.
PMID: 37782247
PMC: 10630848.
DOI: 10.1021/acs.jmedchem.3c01192.
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Calame D, Guo T, Wang C, Garrett L, Jolly A, Dawood M
Am J Hum Genet. 2023; 110(8):1394-1413.
PMID: 37467750
PMC: 10432148.
DOI: 10.1016/j.ajhg.2023.06.013.
G-quadruplexes and associated proteins in aging and Alzheimer's disease.
Vijay Kumar M, Morales R, Tsvetkov A
Front Aging. 2023; 4:1164057.
PMID: 37323535
PMC: 10267416.
DOI: 10.3389/fragi.2023.1164057.
A transposase-derived gene required for human brain development.
Zapater L, Lewis S, Gutierrez R, Yamada M, Rodriguez-Fos E, Planas-Felix M
bioRxiv. 2023; .
PMID: 37163102
PMC: 10168387.
DOI: 10.1101/2023.04.28.538770.
Structure-forming CAG/CTG repeats interfere with gap repair to cause repeat expansions and chromosome breaks.
Polleys E, Del Priore I, Haber J, Freudenreich C
Nat Commun. 2023; 14(1):2469.
PMID: 37120647
PMC: 10148874.
DOI: 10.1038/s41467-023-37901-2.
Recruitment of RBM6 to DNA Double-Strand Breaks Fosters Homologous Recombination Repair.
Awwad S, Darawshe M, Machour F, Arman I, Ayoub N
Mol Cell Biol. 2023; 43(3):130-142.
PMID: 36941773
PMC: 10038030.
DOI: 10.1080/10985549.2023.2187105.
Heavy metal ions exchange driven protein phosphorylation cascade functions in genomic instability in spermatocytes and male infertility.
Li R, Yang D, He Y, Zhou Y, Li C, Li L
Nucleic Acids Res. 2023; 51(7):3150-3165.
PMID: 36869674
PMC: 10123093.
DOI: 10.1093/nar/gkad128.
Neural Tube Defects and Folate Deficiency: Is DNA Repair Defective?.
Wang X, Yu J, Wang J
Int J Mol Sci. 2023; 24(3).
PMID: 36768542
PMC: 9916799.
DOI: 10.3390/ijms24032220.
Epigenomic signatures associated with spontaneous and replication stress-induced DNA double strand breaks.
Kodali S, Meyer-Nava S, Landry S, Chakraborty A, Rivera-Mulia J, Feng W
Front Genet. 2022; 13:907547.
PMID: 36506300
PMC: 9730818.
DOI: 10.3389/fgene.2022.907547.
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Luquette L, Miller M, Zhou Z, Bohrson C, Zhao Y, Jin H
Nat Genet. 2022; 54(10):1564-1571.
PMID: 36163278
PMC: 9833626.
DOI: 10.1038/s41588-022-01180-2.
SIAH2 regulates DNA end resection and replication fork recovery by promoting CtIP ubiquitination.
Jeong S, Hariharasudhan G, Kim M, Lim J, Jung S, Choi E
Nucleic Acids Res. 2022; 50(18):10469-10486.
PMID: 36155803
PMC: 9561274.
DOI: 10.1093/nar/gkac808.
Increased Gene Targeting in Hyper-Recombinogenic LymphoBlastoid Cell Lines Leaves Unchanged DSB Processing by Homologous Recombination.
Mladenov E, Paul-Konietzko K, Mladenova V, Stuschke M, Iliakis G
Int J Mol Sci. 2022; 23(16).
PMID: 36012445
PMC: 9409177.
DOI: 10.3390/ijms23169180.